HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl 3-(bromophenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | (3-Bromophenyl)acetic acid | HCID 74653 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 3-(bromophenyl)acetate | HCID 11470552 | — |
Reaction Steps
To a solution of 2-(3-bromophenyl)acetic acid 1103 (10.0 g, 46.5 mmol) in 100 mL EtOH was added conc. H2SO4 (10 drops) and the mixture heated to relux temperature for 3 hours. The mixture was allowed to cool to room temperature and the volatiles were removed under reduced pressure. The residue was taken up in EtOAc (100 mL) and washed with water (2×50 mL), saturated NaHCO3 (1×25 mL), brine (2×25 mL) and dried over Na2SO4. The Na2SO4 was removed by filtration and the volatiles removed under reduced pressure to give ethyl 2-(3-bromophenyl)acetate 1097 (11.1 grams) as a liquid). 1H NMR 300 MHz CDCl3: δ 7.41 (m, 2H), 7.20 (m, 2H), 4.14 (q, 2H, J=9.5 Hz), 3.57 (s, 2H), 1.25 (t, 3H, J=9.5 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08865718B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-8b4f435480824361a672da04094cbb75 |
| Source note | uspto-grants-2014_10 |